Addressing SARS-CoV-2 evolution: neutralization of emerging variants of concern by the AVX/COVID-12 'Patria' vaccine based on HexaPro-S ancestral Wuhan spike or its updated BA.2.75.2 version.

应对 SARS-CoV-2 的演变:AVX/COVID-12“Patria”疫苗基于 HexaPro-S 祖先武汉刺突蛋白或其更新的 BA.2.75.2 版本,可中和令人担忧的新出现的变异株

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作者:Carballo-Uicab Gregorio, Mellado-Sánchez Gabriela, González-González Edith, Salinas-Trujano Juana, Mendoza-Salazar Ivette, López-Olvera Karina, Gómez-Castellano Keyla M, Salazar Ma Isabel, Torres-Flores Jesús M, Chagoya-Cortés Héctor Elías, Paz-De la Rosa Georgina, Mena Ignacio, Rojas-Martínez Oscar, Lara-Puente Jesús Horacio, Peralta-Sánchez Gustavo Javier, Sarfati-Mizrahi David, Torres-Flores Alejandro, Sun Weina, Krammer Florian, García-Sastre Adolfo, Palese Peter, López-Macías Constantino, Lozano-Dubernard Bernardo, Pérez-Tapia Sonia M, Almagro Juan C
INTRODUCTION: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) remains a global health challenge, causing severe morbidity and mortality, particularly in vulnerable groups such as the elderly, immunocompromised individuals, and those with comorbidities. In low- and middle-income countries (LMICs), vaccine access is hindered by high costs and inequitable distribution. To tackle these issues, Mexico developed the AVX/COVID-12 (V-Wu) vaccine, a recombinant Newcastle disease virus (NDV)-based platform expressing a stabilized ancestral Wuhan spike protein (HexaPro-S). Locally manufactured after rigorous testing and regulatory approval, V-Wu aims to enhance self-sufficiency and equity in immunization. METHODS: This study evaluates an updated vaccine version, AVX/COVID-12 (V-BA), designed to combat Omicron subvariants by expressing the HexaPro-S protein of BA.2.75.2. Both vaccines were administered intramuscularly in K18-hACE2 transgenic and BALB/c mouse models using a prime-boost regimen. Immunogenicity was analyzed by measuring antibodies against Omicron S proteins BA.2.75.2 and XBB.1.5, as well as neutralizing antibodies against Wuhan, BA.1, XBB.1.16, and JN.1 variants. RESULTS: Both vaccines were safe, eliciting robust antibody responses against Omicron S proteins and neutralizing antibodies against multiple emerging SARS-CoV-2 variants of concern (VOCs). V-BA demonstrated superior protection against current Omicron variants, while V-Wu offered broader coverage, including the ancestral Wuhan strain and emerging variants like JN.1. DISCUSSION: These findings underscore the adaptability of NDV-based platforms in addressing the evolving SARS-CoV-2 landscape and reaffirm the ongoing utility of the ancestral Patria vaccine. Together, they demonstrate the potential of these platforms to drive the development of next-generation vaccines tailored to emerging viral threats, contributing to global health equity.

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